The Michaelis constant of enzyme reaction at present condition was calculated.

计算了该实验条件下酶反应的米氏常数.

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The purity of isoquercitrin was isolated with a gel column.

酶反应产物用硅胶柱层析法提取,可以得到高纯度的异槲皮甙.

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The optimum pH was 7.0 for GL - 7 - ACA acylase.

GL -7-ACA 酰化酶反应最适pH为7.0.

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VTT also laccases intercomparsion reaction catalyzed by enzymes, non - ferrous products of indicator for leakage.

VTT也 利用漆酶催化促酶反应形成有色产物,研究渗漏指示剂的构成.

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But the enzyme reaction was far too inefficient to make large scale conversion practical.

但是酶反应效率太低,不足以转化实际需要的大量血液.

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Perform the glucose oxidase reaction, to the glucose sample ( unknown concentration ), according to scheme.

按照下表所示, 加入未知浓度的葡萄糖样本, 针对新的样本,使用相同的葡萄糖氧化酶反应.

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The α - galactosidase has an optimum pH of 5.0 and an optimum temperature of 45℃.

该α - 半乳糖苷酶反应的最适pH为5.0,最适温度为45℃.

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Dot - IGSS, similar to Dot - ELISA, is easy to manipulate and the result is easy to interpret.

与Dot - ELISA相比,Dot - IGSS具有 操作简便 、 容易判断结果等优点, 还具有更高的敏感性和特异性,且不使用酶反应底物.

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